ENST00000346342.8:c.1306G>C
MANE Select
|
ENSP00000329546.4:p.Gly436Arg
|
|
ENST00000346342.7:c.1306G>C
|
ENSP00000329546.3:p.Gly436Arg
|
|
ENST00000375581.3:c.1372G>C
|
ENSP00000364731.3:p.Gly458Arg
|
|
ENST00000541084.5:c.1120G>C
|
ENSP00000442051.2:p.Gly374Arg
|
|
NM_000131.4:c.1372G>C , LRG_554t1:c.1372G>C
|
NP_000122.1:p.Gly458Arg
|
|
NM_001267554.1:c.1120G>C
|
NP_001254483.1:p.Gly374Arg
|
|
NM_019616.3:c.1306G>C , LRG_554t2:c.1306G>C
|
NP_062562.1:p.Gly436Arg
|
|
NR_051961.1:n.1393G>C
|
|
|
XM_006719963.2:c.1165G>C
|
XP_006720026.1:p.Gly389Arg
|
|
XM_011537474.1:c.1414G>C
|
XP_011535776.1:p.Gly472Arg
|
|
XM_011537475.1:c.1228G>C
|
XP_011535777.1:p.Gly410Arg
|
|
XM_011537476.1:c.1066G>C
|
XP_011535778.1:p.Gly356Arg
|
|
XM_011537477.1:c.1375G>C
|
XP_011535779.1:p.Gly459Arg
|
|
XM_006719963.3:c.1210G>C
|
XP_006720026.2:p.Gly404Arg
|
|
XM_011537474.2:c.1459G>C
|
XP_011535776.2:p.Gly487Arg
|
|
XM_011537475.2:c.1273G>C
|
XP_011535777.2:p.Gly425Arg
|
|
XM_011537476.2:c.1066G>C
|
XP_011535778.1:p.Gly356Arg
|
|
NM_019616.4:c.1306G>C
MANE Select
|
NP_062562.1:p.Gly436Arg
|
|
NR_051961.2:n.1390G>C
|
|
|
NM_001267554.2:c.1120G>C
|
NP_001254483.1:p.Gly374Arg
|
|